ES2262504T3 - DERIVATIVES OF THE PYROGLUTAMIC ACID AND RELATED COMPOUNDS THAT INHIBIT THE ADHESION OF LEUKOCYTES THROUGH THE VLA-4. - Google Patents
DERIVATIVES OF THE PYROGLUTAMIC ACID AND RELATED COMPOUNDS THAT INHIBIT THE ADHESION OF LEUKOCYTES THROUGH THE VLA-4.Info
- Publication number
- ES2262504T3 ES2262504T3 ES00904486T ES00904486T ES2262504T3 ES 2262504 T3 ES2262504 T3 ES 2262504T3 ES 00904486 T ES00904486 T ES 00904486T ES 00904486 T ES00904486 T ES 00904486T ES 2262504 T3 ES2262504 T3 ES 2262504T3
- Authority
- ES
- Spain
- Prior art keywords
- substituted
- cycloalkyl
- heterocyclic
- heteroaryl
- aryl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
- C07K5/06173—Dipeptides with the first amino acid being heterocyclic and Glp-amino acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
- C07K5/06165—Dipeptides with the first amino acid being heterocyclic and Pro-amino acid; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06191—Dipeptides containing heteroatoms different from O, S, or N
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Pulmonology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Cardiology (AREA)
- Obesity (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Hematology (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Utilización de un compuesto de la fórmula I o II en donde R1 se selecciona del grupo formado por alquilo, alquilo sustituido, arilo, arilo sustituido, cicloalquilo, cicloalquilo sustituido, heterocíclico, heterocíclico sustituido, heteroarilo y heteroarilo sustituido; R2 se selecciona del grupo formado por alquileno con 2 a 4 átomos de carbono en la cadena alquileno, alquileno sustituido con 2 a 4 átomos de carbono en la cadena alquileno, heteroalquileno con 1 a 3 átomos de carbono y 1 a 2 heteroátomos seleccionados entre nitrógeno, oxígeno y azufre y con 2 a 4 átomos en la cadena heteroalquileno y heteroalquileno sustituido con, en la cadena heteroalquileno, 1 a 3 átomos de carbono y 1 a 2 heteroátomos seleccionados entre nitrógeno, oxígeno y azufre y con 2 a 4 átomos en la cadena heteroalquileno; R3 se selecciona del grupo formado por hidrógeno, alquilo, alquilo sustituido, cicloalquilo, cicloalquilo sustituido, cicloalquenilo, cicloalquenilo sustituido, arilo, arilo sustituido, heteroarilo, heteroarilo sustituido, heterocíclico, heterocíclico sustituido o R3 se puede unir a R2 para formar un anillo fusionado de cicloalquilo, cicloalquilo sustituido, cicloalquenilo o cicloalquenilo sustituido; X se selecciona del grupo formado por hidrógeno, alquilo, alquilo sustituido, cicloalquilo, cicloalquilo sustituido, alcoxilo, alcoxilo sustituido, arilo, arilo sustituido, ariloxilo, ariloxilo sustituido, ariloxiarilo, ariloxiarilo sustituido, heteroarilo, heteroarilo sustituido, heterocíclico, heterocíclico sustituido, acilamino, carboxilo, carboxilalquilo, carboxilalquilo sustituido, carboxilcicloalquilo, carboxilcicloalquilo sustituido, carboxilarilo, carboxilarilo sustituido, carboxilheteroarilo, carboxilheteroarilo sustituido, carboxiheterocíclico, carboxiheterocíclico sustituido e hidroxilo con la condición de que en la fórmula II, X no es hidroxilo; W es oxígeno o azufre; o una sal farmacéuticamente aceptable de los mismos, en la elaboración de un medicamento para usar en el tratamiento de un paciente mamífero de una enfermedad inflamatoria mediada por VLA-4.Use of a compound of the formula I or II wherein R 1 is selected from the group consisting of alkyl, substituted alkyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, heterocyclic, substituted heterocyclic, heteroaryl and substituted heteroaryl; R2 is selected from the group consisting of alkylene with 2 to 4 carbon atoms in the alkylene chain, alkylene substituted with 2 to 4 carbon atoms in the alkylene chain, heteroalkylene with 1 to 3 carbon atoms and 1 to 2 heteroatoms selected from nitrogen , oxygen and sulfur and with 2 to 4 atoms in the heteroalkylene and heteroalkylene chain substituted with, in the heteroalkylene chain, 1 to 3 carbon atoms and 1 to 2 heteroatoms selected from nitrogen, oxygen and sulfur and with 2 to 4 atoms in the heteroalkylene chain; R3 is selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkenyl, substituted cycloalkenyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic or R3 can be attached to R2 to form a fused ring of cycloalkyl, substituted cycloalkyl, cycloalkenyl or substituted cycloalkenyl; X is selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, alkoxy, substituted alkoxy, aryl, substituted aryl, aryloxy, substituted aryloxy, aryloxyaryl, substituted aryloxyaryl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, acylamino , carboxyl, carboxylalkyl, substituted carboxylalkyl, carboxycycloalkyl, substituted carboxycycloalkyl, carboxylaryl, substituted carboxylaryl, carboxyheteroaryl, substituted carboxyheteroaryl, carboxyheterocyclic, substituted carboxyheterocyclic and hydroxyl with the condition X in the hydroxyl with the condition X in hydroxyl; W is oxygen or sulfur; or a pharmaceutically acceptable salt thereof, in the preparation of a medicament for use in the treatment of a mammalian patient of an inflammatory disease mediated by VLA-4.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23866199A | 1999-01-26 | 1999-01-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2262504T3 true ES2262504T3 (en) | 2006-12-01 |
Family
ID=22898814
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES00904486T Expired - Lifetime ES2262504T3 (en) | 1999-01-26 | 2000-01-21 | DERIVATIVES OF THE PYROGLUTAMIC ACID AND RELATED COMPOUNDS THAT INHIBIT THE ADHESION OF LEUKOCYTES THROUGH THE VLA-4. |
Country Status (12)
| Country | Link |
|---|---|
| EP (2) | EP1612215A1 (en) |
| JP (1) | JP2002535341A (en) |
| CN (1) | CN1195773C (en) |
| AR (1) | AR022405A1 (en) |
| AT (1) | ATE323102T1 (en) |
| AU (1) | AU2623800A (en) |
| CA (1) | CA2358093A1 (en) |
| DE (1) | DE60027268T2 (en) |
| ES (1) | ES2262504T3 (en) |
| HK (1) | HK1046146B (en) |
| TW (1) | TWI224110B (en) |
| WO (1) | WO2000043413A2 (en) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2623800A (en) * | 1999-01-26 | 2000-08-07 | American Home Products Corporation | Pyroglutamic acid derivatives and related compounds which inhibit leukocyte adhesion mediated by vla-4 |
| US6407066B1 (en) * | 1999-01-26 | 2002-06-18 | Elan Pharmaceuticals, Inc. | Pyroglutamic acid derivatives and related compounds which inhibit leukocyte adhesion mediated by VLA-4 |
| JP5401218B2 (en) * | 2009-09-03 | 2014-01-29 | 東京応化工業株式会社 | Resist composition and resist pattern forming method |
| CN108299218A (en) * | 2017-01-12 | 2018-07-20 | 南京红杉生物科技有限公司 | A kind of synthetic method of the bromo- D-phenylalanines of 4- |
| CN109180552B (en) * | 2018-09-26 | 2021-10-26 | 沈阳药科大学 | Substituted 5-oxo pyrrolidine derivative and preparation method and application thereof |
| CA3116769C (en) | 2018-10-30 | 2023-08-22 | Gilead Sciences, Inc. | Quinoline derivatives as alpha4beta7 integrin inhibitors |
| WO2020092383A1 (en) | 2018-10-30 | 2020-05-07 | Gilead Sciences, Inc. | Compounds for inhibition of alpha 4 beta 7 integrin |
| CN112969700B (en) | 2018-10-30 | 2024-08-20 | 吉利德科学公司 | Imidazopyridine derivatives as alpha 4 beta 7 integrin inhibitors |
| US11179383B2 (en) | 2018-10-30 | 2021-11-23 | Gilead Sciences, Inc. | Compounds for inhibition of α4β7 integrin |
| WO2021030438A1 (en) | 2019-08-14 | 2021-02-18 | Gilead Sciences, Inc. | Compounds for inhibition of alpha 4 beta 7 integrin |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2193508A1 (en) * | 1994-07-11 | 1996-01-25 | Eugene D. Thorsett | Inhibitors of leukocyte adhesion |
| DE69715860T2 (en) * | 1996-06-21 | 2003-08-07 | Takeda Chemical Industries, Ltd. | METHOD FOR PRODUCING PEPTIDES |
| KR20010022406A (en) * | 1997-07-31 | 2001-03-15 | 진 엠. 듀발 | Dipeptide and related compounds which inhibit leukocyte adhesion mediated by VLA-4 |
| TW591026B (en) * | 1998-06-23 | 2004-06-11 | Upjohn Co | Inhibitors of alpha4beta1 mediated cell adhesion |
| AU2623800A (en) * | 1999-01-26 | 2000-08-07 | American Home Products Corporation | Pyroglutamic acid derivatives and related compounds which inhibit leukocyte adhesion mediated by vla-4 |
-
2000
- 2000-01-21 AU AU26238/00A patent/AU2623800A/en not_active Abandoned
- 2000-01-21 ES ES00904486T patent/ES2262504T3/en not_active Expired - Lifetime
- 2000-01-21 JP JP2000594829A patent/JP2002535341A/en not_active Withdrawn
- 2000-01-21 EP EP05019666A patent/EP1612215A1/en not_active Withdrawn
- 2000-01-21 AT AT00904486T patent/ATE323102T1/en not_active IP Right Cessation
- 2000-01-21 CA CA002358093A patent/CA2358093A1/en not_active Abandoned
- 2000-01-21 EP EP00904486A patent/EP1144435B1/en not_active Expired - Lifetime
- 2000-01-21 WO PCT/US2000/001537 patent/WO2000043413A2/en active IP Right Grant
- 2000-01-21 CN CNB00803107XA patent/CN1195773C/en not_active Expired - Fee Related
- 2000-01-21 DE DE60027268T patent/DE60027268T2/en not_active Expired - Fee Related
- 2000-01-24 AR ARP000100291A patent/AR022405A1/en unknown
- 2000-01-25 TW TW089101188A patent/TWI224110B/en not_active IP Right Cessation
-
2002
- 2002-09-20 HK HK02106863.9A patent/HK1046146B/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE60027268T2 (en) | 2007-03-15 |
| TWI224110B (en) | 2004-11-21 |
| CN1344274A (en) | 2002-04-10 |
| CN1195773C (en) | 2005-04-06 |
| HK1046146A1 (en) | 2002-12-27 |
| ATE323102T1 (en) | 2006-04-15 |
| AR022405A1 (en) | 2002-09-04 |
| EP1612215A1 (en) | 2006-01-04 |
| CA2358093A1 (en) | 2000-07-27 |
| AU2623800A (en) | 2000-08-07 |
| WO2000043413A2 (en) | 2000-07-27 |
| HK1046146B (en) | 2005-07-29 |
| DE60027268D1 (en) | 2006-05-24 |
| EP1144435A2 (en) | 2001-10-17 |
| EP1144435B1 (en) | 2006-04-12 |
| JP2002535341A (en) | 2002-10-22 |
| WO2000043413A3 (en) | 2000-11-30 |
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